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Class ITerminated in FDA datasetRecall initiated Oct 22, 2013

Reser's Fine Foods, Cheesy Macaroni Salad, Formula MA.66 packaged in 12/454-gm carton cases (

Recalling firm: Reser's Fine Foods, Inc.

Why it was recalled

The recalled products are potentially contaminated with Listeria monocytogenes.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 24, 2017.

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Compare the exact product and package details with the label you have.

ProductReser's Fine Foods, Cheesy Macaroni Salad, Formula MA.66 packaged in 12/454-gm carton cases (UPC 071117182415) and 6/1.25-KG carton cases (UPC 071117612271) plastic containers. Reser's Fine Foods, Inc., Beaverton, OR.
UPC071117182415, 071117612271

FDA code information

Use by date 10/20/13 and 12/01/13.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Reser's Fine Foods, Cheesy Macaroni Salad, Formula MA.66 packaged in 12/454-gm carton cases (UPC 071117182415) and 6/1.25-KG carton cases (UPC 071117612271) plastic containers. Reser's Fine Foods, Inc., Beaverton, OR.

Extracted codes and context

TypeCode / valueContext
UPC071117182415s, Cheesy Macaroni Salad, Formula MA.66 packaged in 12/454-gm carton cases (UPC 071117182415) and 6/1.25-KG carton cases (UPC 071117612271) plastic containers. Reser's Fine Foods, Inc., Beaverton, OR.
UPC071117612271ed in 12/454-gm carton cases (UPC 071117182415) and 6/1.25-KG carton cases (UPC 071117612271) plastic containers. Reser's Fine Foods, Inc., Beaverton, OR.

Original FDA recall reason

The recalled products are potentially contaminated with Listeria monocytogenes.

Recall details

Recall number
F-0232-2014
Event ID
66563
FDA status
Terminated
Initiated
Oct 22, 2013
Reported
Jan 1, 2014
Classified
Dec 24, 2013
Terminated
Jan 24, 2017
Quantity
N/A
Location
Beaverton, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distribution was made to AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, WI, WV AND WY. Distribution was also made to Canada.

FDA source record · F-0232-2014

Data updated September 16, 2026. View official FDA data ↗

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